Class II
Terminated
5% Lidocaine HCl and 7.5% Dextrose Injection, USP, 2 mL Single Dose Ampuls, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4712-01
This recall has been terminated (originally issued October 9, 2013).
- Company
- Hospira Inc.
- Recall Initiated
- August 29, 2013
- Posted
- October 9, 2013
- Recall Number
- D-66201-001
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 86,400 ampuls
- Firm Location
- Lake Forest, IL, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Presence of Particulate Matter; report of visible particulates in the glass ampule
Distribution
Nationwide
Lot / Code Info
Lot 23-227-DK
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